Synthesis of 2-Oxindole Derivatives via the Intramolecular Heck Reaction on Solid Support
β Scribed by Vijayalaksmi Arumugam; Anne Routledge; Chris Abell; Shankar Balasubramanian
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 523 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Solid phase intramolecularHeck couplingallows the syothesisof 2-oxindoles. Additional diversityis introducedinfo the moleculeby reductiveatkylationprior to the Heck cyclisationarrdatso by conjugateadditionof a varietyof nucleophilesontothe cyctisedproductprior to cleavage. 01997 Elsevier ScienceLtd.
π SIMILAR VOLUMES
The palladium(0)-catalyzed reaction of derivatives of g-amino-a,b-unsaturated esters bearing an N-(2-iodobenzoyl) substituent results in an intramolecular Heck reaction, the outcome of which depends on the structure of the substrate as well as on the experimental conditions. The methodology develope
## Abstract A Pdβcatalyzed ligandβfree intramolecular Heck coupling of appropriately substituted pyrimidinediones (III) is developed.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v